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Post Surgically Treated Peritonitis Complications

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03284476
Recruitment Status : Withdrawn (No inclusion)
First Posted : September 15, 2017
Last Update Posted : June 4, 2020
Sponsor:
Information provided by (Responsible Party):
Nantes University Hospital

Brief Summary:

The purpose of this observational study is to investigate the management and the complications associated wtih surgically treated peritonitis.

Data will be analysed to answer pre-defined scientific projects and to improve management of these conditions.


Condition or disease Intervention/treatment
Peritonitis Other: Collection of medical data from ICU patients

Detailed Description:
Anonymous data will be collected by study coordinators in a secured e-database. Cross audit will be performed to check data.

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Study Type : Observational
Actual Enrollment : 0 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: A Prospective Cohort of Patients Hospitalized in West French Intensive Care Units for Peritonitis Surgically Treated
Estimated Study Start Date : April 2013
Actual Primary Completion Date : June 2020
Actual Study Completion Date : June 2020

Group/Cohort Intervention/treatment
ICU patients
Collection of medical data of Patients with peritonitis (nosocomial or community-acquired) or Patients with post-operative peritonitis
Other: Collection of medical data from ICU patients
Medical data collected on a electronic secured data base




Primary Outcome Measures :
  1. In ICU stay main complications [ Time Frame: Within the first 28 days after ICU admission date ]
    Nosocomial Infections (epidemiology, risk factors, antibiotic susceptibility of pathogens) Organ failures (incidence, risk factors)


Secondary Outcome Measures :
  1. Duration of mechanical ventilation [ Time Frame: In ICU (up to 90 days) ]
  2. ICU length of stay [ Time Frame: In ICU (up to 90 days) ]

Other Outcome Measures:
  1. Death [ Time Frame: In ICU (up to 90 days) ]


Information from the National Library of Medicine

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Ages Eligible for Study:   15 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients hospitalized in ICU for peritonitis surgically treated
Criteria

Inclusion Criteria:

  • Nosocomial surgically treated Peritonitis
  • Or Community-Acquired surgically treated Peritonitis
  • Or Post-operative surgically treated Peritonitis

Exclusion Criteria:

  • Consent withdrawal

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03284476


Locations
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France
Angers University Hospital
Angers, France, 49000
Nantes University Hospital
Nantes, France, 44093
Poitiers University Hospital
Poitiers, France, 86000
Rennes University Hospital
Rennes, France, 35000
Tours University Hospital
Tours, France, 37000
Sponsors and Collaborators
Nantes University Hospital
Investigators
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Study Chair: Karim Asehnoune, MD, PhD Non Affiliated
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Responsible Party: Nantes University Hospital
ClinicalTrials.gov Identifier: NCT03284476    
Other Study ID Numbers: RC12_0207 doublon
First Posted: September 15, 2017    Key Record Dates
Last Update Posted: June 4, 2020
Last Verified: June 2020
Keywords provided by Nantes University Hospital:
Nosocomial Peritonitis
Community-acquired Peritonitis
Post-operative Peritonitis
Additional relevant MeSH terms:
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Peritonitis
Intraabdominal Infections
Infection
Peritoneal Diseases
Digestive System Diseases